Descripción de la oferta
Legit.Health is seeking a Clinical Affairs Manager to own end-to-end clinical evaluation and regulatory documentation for SaMD and AI-based medical devices. You will lead clinical conversations, coordinate a network of experts, and work with Quality, Regulatory, and Product Development teams in a remote environment.You should have 5+ years in clinical trials or regulatory affairs, strong literature review and data analysis skills, and experience with SAP/SAR, CER/PMCF updates, and regulatory
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